Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K210900 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Alphenix INFX-8000C, interventional fluoroscopic x-ray system | 2 | 01/27/2026 | Canon Medical System, USA, INC. |
| INFX-8000C XGCP-930AA TABLE SIDE CONSOLE, INFX-8000C XGCP-930BA TABLE SIDE CONSOLE | 2 | 08/11/2023 | Canon Medical System, USA, INC. |
| The device is an X-ray system that is capable of radiographic and fluoroscopic studies and is used i... | 2 | 02/16/2024 | Canon Medical System, USA, INC. |
| This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional ang... | 2 | 10/08/2025 | Canon Medical System, USA, INC. |
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